Isolation and Determination of Antibacterial Sensitivity Characteristics of Staphylococcus aureus from Lactating Cows in West Shewa Zone, Ethiopia

Staphylococcus (S.) aureus is one of the etiologies of bovine mastitis, hindering milk production and productivity in dairy farms. This study was aimed at assessing the distribution of bovine mastitis and the isolation rate of S. aureus in milked cows of West Shewa Zone. The clinical mastitis was diagnosed by physical methods including observation and palpation, whereas the subclinical mastitis was tested by the California mastitis test (CMT). All of the cows tested for mastitis were aseptically sampled (teat-milk) for bacteriology. The bacterium was primarily identified based on colony characterization, catalase, coagulase tests, and Gram stain reaction. Finally, MALDI-TOF Biotyper confirmed the species. The antibacterial sensitivity characteristics of the isolates to different antibacterial drugs were tested by the disk diffusion method. The drugs were selected based on the frequent usage in veterinary medicine in the study area. By using particular primers, the presence of the resistance (mecA and blaZ), and thermonuclease (nuc) genes were determined by polymerase chain reaction (PCR). The data were analyzed by R statistical software. The associations between the dependent variables (prevalence of mastitis and S. aureus) and the explanatory variables were analysed by chi-square (χ2) and logistic regression tests at a 95% confidence interval (CI). Accordingly, 258 lactating cows were examined, of which 97 (37.6%) were mastitis positive. Of these mastitis positive cows, 59 (60.8%) were subclinical and 38 (39.2%) were clinical. Among the 258 milk samples, 43 (16.7%) were positive for S. aureus. According to the results of the current investigation, subclinical mastitis was significantly more prevalent than clinical mastitis (p < 0.05). The disease was found varied with the lactation stage of the animal, milking with washed hand, udder washing before milking, and tick infestation of the teat. In comparison to animals from farms with lower number of lactating cows, the prevalence of the bacteria was significantly higher in animals managed in farms with large (OR = 12.58, 95% CI = 2.33–68.54, and p < 0.05) and medium (OR = 12.58, 95% CI = 2.33–68.54, and p < 0.05) population of lactating cows per herd. The isoation rate of the bacterium was also found significantly higher in tick-infested cows (OR = 27.69, 95% CI = 9.71–93.01, and p < 0.05) than tick free cows. The antibiogram tests revealed that the isolates resisted penicillin G and tetracycline group drugs (oxytetracycline and tetracycline). Moreover, the nuc gene was confirmed to be present in all of the examined isolates. However, they were not found harboring blaZ and mecA genes. We concluded that S. aureus is sustaining as a main causative agent of bovine mastitis, and they were resistant to the frequently used antibiotics in public and veterinary medicines in the study areas. Therefore, research-based interventions need to be taken in action to combat the pathogen.


Introduction
Te dairy products are among the resources of the livestock sector, which play important domestic economic roles in Ethiopia. However, the production and productivity of milk, which is the raw material for dairy products, are hindered by various factors, among which diseases, feed, and the genetic variety of the animals are the most frequently incriminated [1,2]. Mastitis has been mentioned among the major obstacles to afect the dairy industry by incuring the dairy farms to unnecessary expenses worldwide in general and in developing countries in particular [3].
According to the symptoms, mastitis can be classifed as clinical and subclinical. Te clinical and subclinical mastitis are assigned whether the signs of the disease are determined by a tentative diagnosis or not. Although only the abnormalities of the milk (changes in color and/or consistency) might be determined in the early stage of clinical mastitis. However, when the illness worsens, the udder begins to show signs of infammation, such as swelling, redness, heat, and pain. In subclinical mastitis (SCM), however, only a reduction in milk yield is apparent without obvious observable alteration in milk or udder of the animal; hence, it remains undetected for a long period of time [4]. As a result, SCM has been considered as a more istractive and prevalent type of the disease than clinical mastitis. It has been estimated that SCM alone can cause more than 90% of total milk losses of dairy farms in Ethiopia [2].
Bovine mastitis is caused by either trauma or infections. Bacteria, fungi, and viruses are implicated in causing mastitis in bovines. Among the bacterial pathogens, S. aureus has been detemined to cause mastitis in animals, and food poisoning in dairy products (particularly in yogurt and cheese) [5,6].
One of the unique characteristics of S. aureus in causing mastitis is that it is difcult to cure once it has developed. Tis might be attributed to the fact that, it possesses a wide variety of virulence and pathogenicity factors including quorum sensing, which enable it to escape immune defense mechanisms, and then causes infections in the availability of immune cells [7]. Te other virulence factors include swift development of antibiotic resistance, enterotoxigenicity, and production enzymes such as staphylokinase, lipase, and hemolysins. Te antibiotic resistance development nature of the pathogen might be linked to acquiring mobile genetic elements through gene transfer [6,8]. For example, the methicillin-resistant S. aureus (MRSA) strains of the bacterium have been evolved by acquiring genetic components known as staphylococcal cassette chromosome mec (SCCmec), [9]. SCCmec contains various virulence genes of which mecA, codesfor a modifed penicillin-binding protein (PBP-2a). Since PBP-2a has less afnity for methicillin, mecA positive S. aureus has developed resistance to methicillin which is drug of choice to treat beta-lactam antibiotic resistant S. aureus infections. In addition the genetic cassette may also contain genes encoding resistance to other groups of antibiotics, and various other virulence factors, including enterotoxins [6,8]. Nevertheless, penicillin resistance of S. aureus might be attributed to penicillinase enzyme production. Penicillinase enzyme, which is coded by blaZ gene,is responsibe for the hydrolysis of penicillin and penicillin derivatives by breaking the -lactam ring of penicillin [10][11][12]. Such characteristics of the pathogen might lead to fatal infections caused by the strains because of the lack of alternative antibiotics [6,13].
Furthermore, the thermostability nature of S. aureus is linked with the nuc gene, which encodes the heat-stable enzyme known as thermonuclease. Terefore, nuc genepositive S. aureus can survive in heat-processed foodstufs, and/or the toxins they produce might be thermostable. However, although the nuc gene detection in S. aureus has been conducted for species identifcation [14,15], the nuc gene is not harbored by all strains of S. aureus [6,16].
Terefore, since S. aureus is an important diseasecausing organism in animals and humans through infection or toxin production in foods [6], assessment of the prevalence and antibiotic susceptibility characteristics of the bacterium in lactating cows can play signifcant roles in the application of treatment and control procedures against the pathogen. Te detection of the genes (mecA, blaZ, and nuc) also helps us to have better understanding of the types of antibiotics intended to be used and/or expect the type of enterotoxins produced (if any) by the isolates. Although few previous studies have been conducted in the study area, they have not detected the resistance or the thermonuclease gene in S. aureus. Te current study was, therefore, carried out to isolate, identify, and detect resistance genes in S. aureus.

Study Area.
West Shewa zone is expected to hold the total population of 2,058,700, of whom 1,028,500 are male and 1,030,200 are female. Tere are about 1.23 million cattle, 0.43 million sheep, 0.19 million goats, 0.207 million equines, and 1.2 million chickens reared in the zone ( Figure 1).
For the current study, four districts of the West Shewa zone, namely, Walmara, Ambo, Toke Kutaye, and Bako Tibe, were randomly selected. Te agroecological features, and geographical situations of the districts are illustrated in Table 1.

Study Animal.
Inclusion Criteria: the study included lacating cows of the selected districts. Tat is to be included in the study, the cow should have been lactated at the time samples were collected. Both the local and crossbred cows (crossed between the Zebu and exotic breeds) were included.
Exclusion Criteria: cows, which were not lactating at the sampling time, were excluded from the study.
Te ages of the animals were recorded according to the information obtained from the owners. Te management systems of the farms were assigned based on the criteria set, and judged by observation.

Study Design. Te investigation was conducted between
May 2020 and March 2021 using cross-sectional types of the study design.  [17] earlier formula, the number of animals that were sampled was estimated as follows: where N is for sample size, z is the z value at 95% confdence intervals (1.96), p stands for predicted prevalence, and d stands for absolute precision, which is 0.05 at 95% CI.
Since the earlier studies performed in some localities of the area reported the prevalence of mastitis to be 70.6%, the number of samples was then calculated with the expected prevalence of 0.71. Terefore, a total of 318 animals were expected to be tested for mastitis. However, only 258 animals were checked for mastitis. Te pooled milk samples from all functional teats per animal were collected from all mastitischecked animals for bacteriology.

Sampling
Techniques. Te districts, the peasant associations (PAs) in each district, and the farmers who had lactating cows at the time of sampling were randomly selected using a lottery system. However, since the advanced (semi-intensive and intensive) dairy farms were few in number, all of them were purposefully selected for the study. Te clinical-mastitis-positive animals were sampled purposively. However, randomly chosen cows that did not exhibit obvious indications of infammation on their teats or udders were examined for subclinical mastitis using the California mastitis test (CMT).  Veterinary Medicine International Te number of milked cows in each farm was divided into three categories as: small (1-5 heads), medium (6-10 heads), and large (>10 heads). Te lactating stage of the animals was classifed in such a way that "early" from 0 to 3 months, "mid" from 3 to 6 months, and "late" longer than 6 months since gestation. Te cows were divided into three age groups as: young < 4 years old, medium from 4 to 6 years, and adults > 7 years old. Te cows were also grouped according to their parity level as few (1-2 calving), medium (3-5 calving), and many (>5 calving) [18].
Physical observation and palpation (when needed) of the animal were made to determine the body condition of the animal, tick infestation of the teat area, and presence of clinical mastitis. Te body condition of the animal was recorded as good, moderate, or poor according to the criteria set by Metaferia et al. [19]. Te clinical mastitis was considered as positive whenever there were changes in color and/or consistency of milk, or the cardinal signs of udder infammation were observed.
Te CMT was carried out in accordance with instructions provided by Quinn et al. [20]. Milk from each functional teats was squirted in each CMT paddle cup and then combined with roughly the equal amounts of 3% CMT reagent. Te puddle was moved gently to agitate the mixture. Te production of jelly (viscous) consistency within 3-5 minutes was considered CMT positive and then recorded as subclinical mastitis positive.
Strict aseptic practices were applied to prevent contamination from milker hands, the barn surroundings, and skin of the udder and teats. Briefy, the sample collector's hands were protected with gloves and disinfected with 70% ethanol. Te teat were washed, disinfected with 70% ethanol, and the foremilk (initial jets) was expelled. A milk sample of 3 to 5 mL was drawn into a sterile universal bottle. Te bottle was then labeled (with the animal ID, district, and the date of collection), and transported to the laboratory (Zoonosis and Food Safety Research Laboratory of Ambo University). Te milk samples for bacteriology were collected as the pooled sample that milk from all functional quarters of a cow was squirtedinto a single test tube for bacterial identifcation. Terefore, the prevalence rate of S. aureus was expressed as per cow.

Isolation and Identifcation of S. aureus.
In the laboratory, each sample was enriched with approximately 5 mL of sterile brain heart infusion (BHI) broth and incubated for 24 hours at 37°C. Consequently, the enriched culture was then spread onto a mannitol salt agar (MSA) plate and incubated at 37°C for 24 hours. Bacterial growth and mannitol fermentation within 24 hours were checked. Te single colony was chosen and subcultured on brain-heartinfusion (BHI) agar. Te pure colony on BHI agar was then stained by Gram stain, and observed under a light microscope. Te morphology and arrangements of the bacterial cells was determined. Gram positive (purple blue) cocci with grape-like cellular arrangement were presumptively considered as staphylococci. Primary biochemical tests such as catalase and coagulase tests were carried out on the presumptive isolates [6].
Finally, the suspicious isolates were confrmed as S. aureus by matrix-assisted laser desorption/ionization timeof-fight (MALDI-TOF) Biotyper mass spectrometry using the extended direct transfer (EDT) approach in accordance with the procedure described in Feyissa et al. [6].

Antibiogram Characteristics of S. aureus Isolates.
To assess the isolates' susceptibility to antibacterial agents, we used disk difusion techniques [21]. Initially, the purity of the isolates was checked on BHI agar. Second, 3-4 distinct pure colonies (24 hours culture) were suspended in a sterile 0.85% NaCl solution (to a concentration level of 0.5 McFarland turbidity). Te turbidity was measured by using the McFarland Densitometer. Te cotton swab on wooden stick was deeped into the suspension and streaked onto Muller-Hinton agar plates until the inoculum had sufciently covered the plate's surface. Using a disk dispenser, the antibiotic disks were then applied to the agar plate and incubated at 37°C for 18 hours. Te zones of inhibition of each antibiotic were measured (in mm), and the diameter was compared to the guidelines provided by the CLSI manual [22]. Te drugs were chosen based on their availability in the laboratory and distribution in local veterinary clinics and pharmacies. As a result, the following antibiotics were chosen: (1) Erythromycin (15 mg An equal amount of 2 μl of extracted DNA from each sample and 2 μl of the master mix were mixed separately. Sterile water was used as the negative control. Te specifc primers of mecA, nuc [15], and blaZ [12] (Eurofns Genomic India Pvt. Ltd) were employed to target the oxacillin-resistant, thermonuclease, and penicillinase genes, respectively (Table 1).
Te amplifcation of the genes was carried out in such a way that the above mixture was added to the PCR tubes and labelled gently. Te PCR tubes with all the components were transferred to a Flex cycler thermal cycler (Biometra Gmbh, Germany). Te thermal cycler was programmed as initial denaturation 95°C for 5 min and then the fnal denaturation at 95°C for 30 sec, annealing at 55°C for 30 sec, extension at 72°C for 1 min, and a fnal extension at 72°C for 10 min repeating for 37 cycles [23].

Gel Electrophoresis and Visualization of Amplicons.
Te PCR products that were stained with ethidium bromide were separated by electrophoresis in a 1.5% (w/v) agarose gel. Te PCR product mixed with loading dye (bromophenol blue) was applied in the slots of the agarose gel. A maximum of 600 bp of DNA markers (Qiagen; Germany) with 100 bp interval DNA fragments were used to estimate the length of the amplicons. Electrophoresis was then run for one hour at 120 V with 1X TBE bufer. Te separated PCR products in electrophoresis were then photographed using UV illumination and recorded by a gel documentation system (Gel DocTM XR+, BioRAD; Germany).

Data
Analysis. Data from the feld and lab were collected, coded, and entered into Microsoft Excel 2016 fles.
R statistical analysis software was used to analyze the data. Te association between the dependent variables (the prevalence of mastitis and S. aureus) and the risk factors was determined using the chi-square (χ 2 ) test and univariable and multivariable logistic regressions at 95% confdence intervals and a p value <0.05.

S. aureus Isolation Rate and Risk Factors.
A total of 258 milk samples from lactating cows were collected; 97 (37.6%) of these samples were from mastitis-positive cows, of which 59 (60.82%) were subclinical and 38 (39.5%) were clinical cases.
Out of the total 258 milk samples collected, 43 (16.67%) were S. aureus positive. Te bacterium was isolated at a rate of 34/97 (35.05%) in mastitis-positive animals and 9/161 (5.59%) in mastitis-negative animals. Of the 34 S. aureus isolates from mastitis-positive cows, 19 (55.88%) were from clinical and the rest 15 (44.12%) were from subclinical mastitis. Te chisquare (χ 2 ) test analysis revealed a signifcant correlation between the cows' mastitis positivity and the rate of S. aureus isolation. Similarly, the rate was found signifcantly varied with the type of mastitis that the bacterium was highly signifcant in clinical mastitis compared with subclinical mastitis (p < 0.05). Tis might make it evident that bovine mastitis which is caused by S. aureus is mostly clinical.
Te logistic regression analysis of S. aureus and associated risk factors is displayed in Table 2. Te univariate logistic regression analysis revealed that the districts, farm type, animals' body conditions, number of lactating cows in the herd, washing of the milker's hands and udder before milking, tick infestation, and mastitis positivity were associated signifcantly with the isolation rates of S. aureus. In the analysis of multivariate logistic regression, S. aureus was isolated at a signifcantly higher rate in the animals from farms with a large number of lactating cows in the herd and those infested with ticks than in the animals from farms with a small number of lactating cows and free of tick infestation, respectively (p < 0.05).
Also, we made an efort to identify the prevalence of mastitis and other risk variables among lactating cows in the research area. Out of 258 cows examined, 97 (37.6%) had mastitis, with 38 (39.18%) having clinical mastitis and 59 (60.82%) having subclinical mastitis. Te occurrence rate of the disease was found to signifcantly vary with the farm type, lactation stage, milker's hand washing before milking, udder washing before milking, and current tick infestation of the teat. Hence, the occurrence of the disease was signifcantly higher in mid and late than early lactation stage and in cows managed under an extensive management system than in an intense management system. Furthermore, the disease occurred more frequently in animals milked with unwashed hands than in animals milked with washed hands, in animals whose udders were not washed before milking than in animals washed before milking, and in tick-infested animals than in tick-free animals (p < 0.05) ( Table 3).
Te chi-square test model revealed that SCM was generally signifcantly higher than clinical mastitis in the population. Te disease types were discovered to vary with the age group; current tick infestation of the teat indicated that the animals in the younger age group were developing subclinical mastitis more frequently than the medium-aged groups. Tick-infested teats, on the other hand, were found to develop clinical types of the disease more frequently than tick-free teats (p < 0.05).

Antibiogram Characteristics of S. aureus.
Te antibiotic susceptibility profles of 10 of the 43 S. aureus isolates were examined using 9 antibiotic disks. In the current study susceptibility of the isolates to Novobiocin was also Veterinary Medicine International   Veterinary Medicine International  (Table 4). Research has also investigated that the antibiotics Penicillin G, ox Tetracyclin, and Trimethoprim/Sulfamethoxazole are the most common drugs used for bovine treatment in the study area.

Antibiotic Resistance and nuc
Genes. Te antibiotic susceptibility tested S. aureus isolates were also checked if they have been harboring the drug resistance genes-blaZ and mecA-e, and thermonuclease (nuc) genes. Te results of the conventional PCR revealed that all the tested S.aureus isolates bore the 279 bp long nuc gene. But none of them were found possessing the 163 bp and 846 bp long mecA and blaZ genes, respectively (Figure 2).
S. aureus isolation rates were also found to difer between clinical and subclinical mastitis, with the pathogen being signifcantly more common in clinical mastitis-positive cows (OR � 2.93) than in subclinical mastitis-positive cows if other variables remained constant. In dissimilarity to the current study, Mekibib et al. [30] and Madut et al. [31] determined a higher S. aureus isolation rate in subclinical than clinical mastitis.
S. aureus has been identifed as one of the primary etiologies of infectious mastitis in cattle [32]. Te bacterium resides on superfcial surfaces of the udder and the teats, as well as in the teat canal [33][34][35]. It is among the microfora and hence sometimes infects the animal as an opportunistic pathogen as the consequence of mechanical injury to the teat and other stress factors [36].
In the current study, increase in the number of lactation cows in the herd and tick infestation were linked with the higher isolation rates of S. aureus. Te number of the lactating cows might afect the hygienic practices such as washing of milker's hands and teats of the animals before milking unless there is an increase in labor resources in the farm. In line with the current fndings, Gebremedhin et al. [37] found a direct correlation between tick infestation and the prevalence rate of S. aureus in milk samples, as well as an inverse correlation between teat washing before milking and the isolation rate of S. aureus. Vouraki et al. [38] also reviewed that there have been reports of S. aureus isolation from Rhipicephalus spp. tick. S. aureus can spread from infected to uninfected udder quarters during milking if the cow's udder or teats are not cleaned before milking since it lives on the udder or teat surface of cows.
Te prevalence of S. aureus did not signifcantly vary across animal parity levels in the current investigation (p > 0.05). Birhanu et al. [2], Garedew et al. [39], and Tasse et al. [40], however, reported the increment of the isolation rate of S. aureus with the parity number of cows.
It has been determined that 37.6% (97/258) of the tested cows were mastitis positive. Tis result was consistent with that of Sarba and Tola [41], who found that the prevalence of bovine mastitis in the Ambo district was 41.7%. However, Dabele et al. [18] found a higher prevalence rate (30.5%) of the disease in selected districts of the zone. Te fndings of most of the previous studies regarding bovine mastitis conducted in other parts of the country have reported the prevalence rate ranging between 46% and 73% which were higher than the current fnding [3, 23, 25-28, 41, 42].
We found that the animals at the medium and late lactation stages were about 5 and 6 times more mastitic, respectively, than the early lactation stage. Similarly, the management systems were found signifcantly afecting the prevalence rate of the disease. Accordingly, the cows managed under an extensive farming system were found Veterinary Medicine International about 8 times more attacked by mastitis than the cows managed under an intensive farming system. Tis might be because the extensive management system exposes the animal to trauma and tick infestation during grazing in the feld, which, in turn, exposes the teats to pathogenic microorganisms including S. aureus. Te rate of isolation of S. aureus in the current study was higher in tick-infested animals (OR = 27.69, 95% CI: 9.71-93.01, and p < 0.001) than in tick free lactating cows. Te fndings are consistent with previous research on the relationship between tick infestation and mastitis in Ethiopian cattle [43][44][45][46]. Te positive association between tick infestation and bovine mastitis has been reported from diferent parts of the world [30,37,46,47]. However, very few research studies, for example, Tolosa et al. [49] and Dabele et al. [18] in Ethiopia, reported that there is no signifcant variation in prevalence mastitis between tick-infested and tick free cows. Since ticks damage the tissues of teats and can be vectors for pathogenic microorganisms, they are strongly associated with udder lesions and mastitis in cattle [50][51][52]. However, little has been understood about the association between the parasite infestation and mastitis in Ethiopia [1]. In this research, lactation stage was found associated with bovine mastitis and the fnding was in accordance with the previous fndings [53,54]. Te fnding agrees with Baraki et al. [55], Etifu and Tilahun [28], Abebe et al. [3], and Sarba and Tola [41] reports. According to Abera et al. [42], the rate of bovine mastitis was higher in cows with above 6 months of lactation than the early lactating cows. Similarly, Abebe et al. [3] and Dabele et al. [18] determined that the animals with early lactation stage have less probability to be afected by mastitis than those in the above middle lactation stage. Kitila et al. [45] and Argaw [53] stated, however, that bovine mastitis is more prevalent in cows with early stage than the middle lactation stages.
In our study, we also determined that washing hands before milking played a signifcant role in reducing mastitis in lactating cows. Our determination agreed with the fnding of Shittu et al. [56] who found that the cows in the farms where hand washing before milking had been practiced were less afected by mastitis than the counterpart. Milker's hands might serve as the main vehicle for the spread of pathogenic microorganisms among the teats of the same animal and/or diferent animals. It is, therefore, crucial that washing hands within the interval of milking each animal can reduce the transmission chances among the animals [3].
Udder washing is an important hygienic practice to reduce not only the contamination of milk by pathogens of animal origin, but it also reduces the distribution of mastitiscausing microorganisms from animal to animal. Washing udders prior to milking can also remove dirt, organic matter, and microorganisms, promote milk let-down, and improve milk quality. Te evidence found in this study confrms the practice to reduce the occurrence of mastitis in bovine. Previous studies also pointed that udder washing was found reducing the prevalence rate of mastitis in bovine [18,30]. In contrast, however, Abebe et al. [3] did not fnd the udder washing associated with the reduction of mastitis in cows. But it should be underlined that the practice is not solely used to prevent mastitis since mastitis is a multifactorial disease in dairy animals [2].
Te costly nature of mastitis in the dairy industry might be attributed to reduction in milk yield and quality and increment of treatment costs [2,3,27,28]. Te disease can also afect the responses of the ovarian follicules in cows as a consequence of which the conception rate can signifcantly decrease [57].
Furthermore, we have found that subclinical mastitis was signifcantly prevalent than the clinical type of the disease in the study area. About 61% of the mastitis-positive cows were  Figure 2: UV-illuminator imaged PCR product after electrophoresis in 1.5% agarose gel. L � ladder, S1-S10 denote samples, and NC stands for negative control. Description: the length of mecA � 163 bp, nuc � 279 bp, and blaZ � 846 bp. Note: bp represents base pairs. Veterinary Medicine International 9 subclinical, and the rest 39% were clinical mastitis (p < 0.05). It has been reported that subclinical mastitis is the more common type of the disease than clinical mastitis [2]. In this aspect, the current fnding is in accordance with the fndings of most studies [29,[57][58]. Argaw [53] estimated the prevalence of clinical and the subclinical mastitis in Ethiopia to be 23 and 85%, respectively. Te occurrence rate of clinical mastitis in this study was 14.73% (38/258), which is greater than the rates reported by Abera et al. [42] (10%), Abebe et al. [3] (3.4%), and Bekele et al. [27] (10%). Te prevalence rate of subclinical mastitis (26.81%) is less than the reports of Abera et al. [42], Abebe et al. [3], Birhanu et al. [2], Baraki et al. [55], and Bekele et al. [27] who have reported the rates as 36.7%, 59.2%, 40%, 45.5%, and 47%, respectively. All the 10 isolates checked for the antibiotic susceptibility were determined resistant to the three of the most commonly used drugs in the veterinary drugs in the study area: Tetracycline, Penicillin G, and Oxytetracycline. However, all of the ten S. aureus isolates were susceptible to Trimethoprim/Sulfamethoxazole, Gentamycin, Ciprofoxacin, Erythromycin, Clindamycin and. Cefoxitin, Te observational analysis revealed that Pen-streptomycine, Penicillin G, Oxytetracycline, and sulfa drugs such as Sulfadimidine and Trimethoprim/Sulfamethoxazole are the most commonly used antibiotics in veterinary medicine. Te disadvantages of using the sulfa drug as a treatment in practical applications are that they are needed in high doses and are less efective against infammation-causing infections. Te current study is in line with the assessments of Bekele et al. [27], Seyoum et al. [26], Mekonnen et al. [60], and Girmay et al. [61] who determined majority of mastitis cows isolated S. aureus resistant to Oxytetracycline and/or. Penicillin G.
Te augmentation of the resistance pattern of the mastitis-causing microbes including S.aureus to commonly used antibiotics poses an additional burden on the industry [3]. It should also be underlined that the resistant microorganisms obtained locally can be disseminated to another area through the transportation of food materials.
All the tested isolates have harbored the nuc gene. However, the blaZ gene was not observed although the isolates were 100% Penicillin G resistant. BlaZ gene is responsible for hydrolysing the beta-lactam antibiotics such as penicillin and ampicillin because it encodes the β-lactamase enzyme [62]. Te lack of mecA in the isolates was confrmation for susceptibility of the S. aureus isolates to cefoxitin, and the availability of nuc indicated that the isolates were thermostable [62].

Conclusions
Based on the study's fndings, we deduced that S. aureus continues to be the primary cause of mastitis in dairy cows. Clinical mastitis was shown to have a greater prevalence of S. aureus than subclinical mastitis. Also, it was discovered that the study area has a high distribution of bovine mastitis. Te antibacterial susceptibility traits of S. aureus showed us that they were extremely resistant to the locally prevalent antibiotics used in veterinary cares. Tere may be other genetic components or methods by which the bacteria resist penicillin, which could account for the absence of the blaZ gene in the examined S. aureus isolates. Terefore, the prevention and control of the pathogen, and as a consequence, the reduction of the prevalence of the disease, need to be designed. Antibiotics with better treatment responses should also be introduced to the area. Furthermore, the penicillin-resistant mechanism of S. aureus should be studied in depth.

Data Availability
Te data used to support the fndings of the study are available on request from the corresponding author.

Conflicts of Interest
Te authors declare that they have no conficts of interest.